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Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress
INTRODUCTION: A growing body of evidence suggests that stress is an important factor in depression, and pro‐inflammatory cytokines contribute to the occurrence and development of depression in both animal models and human patients. Toll‐like receptor 4 (TLR4) has been shown to be a key innate immune...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066327/ https://www.ncbi.nlm.nih.gov/pubmed/31945269 http://dx.doi.org/10.1002/brb3.1525 |
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author | Zhang, Ke Lin, Wenjuan Zhang, Juntao Zhao, Yawei Wang, Xiaqing Zhao, Mei |
author_facet | Zhang, Ke Lin, Wenjuan Zhang, Juntao Zhao, Yawei Wang, Xiaqing Zhao, Mei |
author_sort | Zhang, Ke |
collection | PubMed |
description | INTRODUCTION: A growing body of evidence suggests that stress is an important factor in depression, and pro‐inflammatory cytokines contribute to the occurrence and development of depression in both animal models and human patients. Toll‐like receptor 4 (TLR4) has been shown to be a key innate immune pattern recognition receptor involved in the regulation of stress responses and inflammation. However, the exact effects of TLR4 on depressive‐like behaviors induced by chronic social defeat stress (CSDS) are not known. METHODS: In this study, the effects of TLR4 on depressive‐like behaviors were investigated in an animal model of depression induced by CSDS. The depressive‐like behaviors were assessed by forced swimming test (FST), social interaction test (SIT), and light–dark box test (LDT). The protein expressions of TLR4 and tumor necrosis factor‐α (TNF‐α) in the hippocampus were measured using Western blotting. RESULTS: We found that CSDS increased TLR4 protein levels in the hippocampus and induced behavioral despair in FST, social avoidance in SIT, and anxiety‐like behavior in LDT. Fluoxetine normalized the increased expression of TLR4 and reversed behavioral despair, social avoidance, as well as anxiety‐like behavior induced by CSDS. However, directly blocking TLR4, by using either TLR4 inhibitor TAK‐242 or knockout of TLR4, only inhibited behavioral despair, but not social avoidance or anxiety‐like behavior induced by CSDS. CONCLUSIONS: These results demonstrate a specific modulating role of TLR4 in behavioral despair induced by CSDS and suggest that TAK‐242 may be a beneficial treatment for patients with behavioral despair. |
format | Online Article Text |
id | pubmed-7066327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70663272020-03-18 Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress Zhang, Ke Lin, Wenjuan Zhang, Juntao Zhao, Yawei Wang, Xiaqing Zhao, Mei Brain Behav Original Research INTRODUCTION: A growing body of evidence suggests that stress is an important factor in depression, and pro‐inflammatory cytokines contribute to the occurrence and development of depression in both animal models and human patients. Toll‐like receptor 4 (TLR4) has been shown to be a key innate immune pattern recognition receptor involved in the regulation of stress responses and inflammation. However, the exact effects of TLR4 on depressive‐like behaviors induced by chronic social defeat stress (CSDS) are not known. METHODS: In this study, the effects of TLR4 on depressive‐like behaviors were investigated in an animal model of depression induced by CSDS. The depressive‐like behaviors were assessed by forced swimming test (FST), social interaction test (SIT), and light–dark box test (LDT). The protein expressions of TLR4 and tumor necrosis factor‐α (TNF‐α) in the hippocampus were measured using Western blotting. RESULTS: We found that CSDS increased TLR4 protein levels in the hippocampus and induced behavioral despair in FST, social avoidance in SIT, and anxiety‐like behavior in LDT. Fluoxetine normalized the increased expression of TLR4 and reversed behavioral despair, social avoidance, as well as anxiety‐like behavior induced by CSDS. However, directly blocking TLR4, by using either TLR4 inhibitor TAK‐242 or knockout of TLR4, only inhibited behavioral despair, but not social avoidance or anxiety‐like behavior induced by CSDS. CONCLUSIONS: These results demonstrate a specific modulating role of TLR4 in behavioral despair induced by CSDS and suggest that TAK‐242 may be a beneficial treatment for patients with behavioral despair. John Wiley and Sons Inc. 2020-01-16 /pmc/articles/PMC7066327/ /pubmed/31945269 http://dx.doi.org/10.1002/brb3.1525 Text en © 2020 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Zhang, Ke Lin, Wenjuan Zhang, Juntao Zhao, Yawei Wang, Xiaqing Zhao, Mei Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress |
title | Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress |
title_full | Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress |
title_fullStr | Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress |
title_full_unstemmed | Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress |
title_short | Effect of Toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress |
title_sort | effect of toll‐like receptor 4 on depressive‐like behaviors induced by chronic social defeat stress |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066327/ https://www.ncbi.nlm.nih.gov/pubmed/31945269 http://dx.doi.org/10.1002/brb3.1525 |
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